DePiero A D, Lourie E M, Berman B W, Robin N H, Zinn A B, Hostoffer R W
Department of Pediatrics, Rainbow Babies and Childrens Hospital, Cleveland, Ohio 44106-5000, USA.
J Pediatr. 1997 Sep;131(3):484-6. doi: 10.1016/s0022-3476(97)80085-6.
We describe two patients with clinical and cytogenetic findings consistent with DiGeorge/velocardiofacial syndrome who had recurrent cytopenias at presentation. Our observations suggest that recurrent cytopenias may be part of the clinical spectrum of deletion 22q11.2. We also suggest that the diagnosis of DG/VCF syndrome be considered in patients with unexplained recurrent immune cytopenias in association with cardiac lesions, subtle craniofacial dysmorphisms, and/or learning or behavioral impairments.
我们描述了两名患者,其临床和细胞遗传学检查结果符合DiGeorge/心脏颜面综合征,在就诊时出现反复血细胞减少。我们的观察结果表明,反复血细胞减少可能是22q11.2缺失临床谱的一部分。我们还建议,对于伴有心脏病变、轻微颅面畸形和/或学习或行为障碍的不明原因反复免疫性血细胞减少患者,应考虑诊断为DG/VCF综合征。